UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk

Epilepsia (Copenhagen), 2018-07, Vol.59 (7), p.1372-1380

2018

Volltextzugriff (PDF)

Both gain‐of‐function and loss‐of‐function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox‐Gastaut syndrome

Epilepsia (Copenhagen), 2019-09, Vol.60 (9), p.1881-1894

2019

Volltextzugriff (PDF)

Epilepsy Surgery in Children

The Pediatric clinics of North America, 2021-08, Vol.68 (4), p.845-856

2021

Volltextzugriff (PDF)

TUBA1A Mutation Associated With Eye Abnormalities in Addition to Brain Malformation

Pediatric neurology, 2015-11, Vol.53 (5), p.442-444

2015

Volltextzugriff (PDF)

Generalizability of High Frequency Oscillation Evaluations in the Ripple Band

Frontiers in neurology, 2018-06, Vol.9, p.510-510

2018

Volltextzugriff (PDF)

Single-center experience with Beta-propeller protein-associated neurodegeneration (BPAN); expanding the phenotypic spectrum

Molecular genetics and metabolism reports, 2019-09, Vol.20, p.100483, Article 100483

2019

Volltextzugriff (PDF)

Interrater Reliability of Visually Evaluated High Frequency Oscillations

Clinical neurophysiology, 2017-03, Vol.128 (3), p.433-441

2017

Volltextzugriff (PDF)

Infraslow status epilepticus: A new form of subclinical status epilepticus recorded in a child with Sturge–Weber syndrome

Epilepsy & behavior, 2015-08, Vol.49, p.193-197

Bello-Espinosa, Luis E

2015

Volltextzugriff (PDF)

Contribution of rare genetic variants to drug response in absence epilepsy

Epilepsy research, 2021-02, Vol.170, p.106537-106537, Article 106537

2021

Volltextzugriff (PDF)

Intravenous Immunoglobulin as a Treatment for Intractable Epilepsy Secondary to Focal Cortical Dysplasia: A Meta-analysis

Pediatric neurology, 2017-11, Vol.76, p.79-81

2017

Volltextzugriff (PDF)

Infraslow EEG changes in infantile spasms

Journal of clinical neurophysiology, 2014-12, Vol.31 (6), p.600-605

2014

Volltextzugriff (PDF)

Outcomes Trajectories in Children With Epilepsy: Hypotheses and Methodology of a Canadian Longitudinal Observational Study

Pediatric neurology, 2014, Vol.50 (1), p.38-48

2014

Volltextzugriff (PDF)

Levetiracetam for benign epilepsy of childhood with centrotemporal spikes—three cases

Seizure (London, England), 2003-04, Vol.12 (3), p.157-159

2003

Volltextzugriff (PDF)

Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child

Archives of ophthalmology (1960), 2007-06, Vol.125 (6), p.840

2007

Volltextzugriff (PDF)

Discontinuation of antiepileptic drugs after successful epilepsy surgery. A Canadian survey

Epilepsy research, 2012-11, Vol.102 (1), p.23-33

2012

Volltextzugriff (PDF)

Epilepsy. Animal and Human Correlations. 2012. By David W. McCandless. Published by Springer. 532pages. C$240 approx

Canadian journal of neurological sciences, 2013-01, Vol.40 (1), p.132-132

Bello-Espinosa, Luis E.

2013

Volltextzugriff (PDF)

Intravenous Immunoglobulin as a treatment for intractable epilepsy secondary to focal cortical dysplasia (P5.243)

Neurology, 2017-04, Vol.88 (16_supplement)

2017

Volltextzugriff (PDF)

Both gain‐of‐function and loss‐of‐function de novo CACNA 1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox‐Gastaut syndrome

Epilepsia (Copenhagen), 2019-09, Vol.60 (9), p.1881-1894

2019

Volltextzugriff (PDF)

Single-center experience with Beta-propeller protein-associated neurodegeneration (BPAN); expanding the phenotypic spectrum

Molecular genetics and metabolism reports, 2019, Vol.20, p.100483-100483

2019

Volltextzugriff (PDF)

Epilepsy. Animal and Human Correlations. 2012. By McCandlessDavid W.. Published by Springer. 532pages. C$240 approx

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2013, Vol.40 (1), p.132-132

Bello-Espinosa, Luis E.

2013

Volltextzugriff (PDF)

Child‐ and parent‐reported quality of life trajectories in children with epilepsy: A prospective cohort study

Epilepsia (Copenhagen), 2017-07, Vol.58 (7), p.1277-1286

2017

Volltextzugriff (PDF)

Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45

Epilepsia (Copenhagen), 2018-01, Vol.59 (1), p.e5-e13

2018

Volltextzugriff (PDF)

Early role for a Na + ,K + -ATPase ( ATP1A3 ) in brain development

Proceedings of the National Academy of Sciences - PNAS, 2021-06, Vol.118 (25), p.1

2021

Volltextzugriff (PDF)

Deficiencia de hierro en enfermedad renal crónica

Revista colombiana de nefrología (En línea), 2023-10, Vol.10 (1)

2023

Volltextzugriff (PDF)

Children's perspective of quality of life in epilepsy

Neurology, 2015-05, Vol.84 (18), p.1830-1837

2015

Volltextzugriff (PDF)

1 – 25 von 29

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(26)
Mit Volltextzugriff
(21)

Publikationsform

Artikel
(27)
Berichte
(1)
Reviews
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk

Both gain‐of‐function and loss‐of‐function de novo CACNA1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox‐Gastaut syndrome

Epilepsy Surgery in Children

TUBA1A Mutation Associated With Eye Abnormalities in Addition to Brain Malformation

Generalizability of High Frequency Oscillation Evaluations in the Ripple Band

Single-center experience with Beta-propeller protein-associated neurodegeneration (BPAN); expanding the phenotypic spectrum

Interrater Reliability of Visually Evaluated High Frequency Oscillations

Infraslow status epilepticus: A new form of subclinical status epilepticus recorded in a child with Sturge–Weber syndrome

Contribution of rare genetic variants to drug response in absence epilepsy

Intravenous Immunoglobulin as a Treatment for Intractable Epilepsy Secondary to Focal Cortical Dysplasia: A Meta-analysis

Infraslow EEG changes in infantile spasms

Outcomes Trajectories in Children With Epilepsy: Hypotheses and Methodology of a Canadian Longitudinal Observational Study

Levetiracetam for benign epilepsy of childhood with centrotemporal spikes—three cases

Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child

Discontinuation of antiepileptic drugs after successful epilepsy surgery. A Canadian survey

Epilepsy. Animal and Human Correlations. 2012. By David W. McCandless. Published by Springer. 532pages. C$240 approx

Intravenous Immunoglobulin as a treatment for intractable epilepsy secondary to focal cortical dysplasia (P5.243)

Both gain‐of‐function and loss‐of‐function de novo CACNA 1A mutations cause severe developmental epileptic encephalopathies in the spectrum of Lennox‐Gastaut syndrome

Single-center experience with Beta-propeller protein-associated neurodegeneration (BPAN); expanding the phenotypic spectrum

Epilepsy. Animal and Human Correlations. 2012. By McCandlessDavid W.. Published by Springer. 532pages. C$240 approx

Child‐ and parent‐reported quality of life trajectories in children with epilepsy: A prospective cohort study

Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45

Early role for a Na + ,K + -ATPase ( ATP1A3 ) in brain development

Deficiencia de hierro en enfermedad renal crónica

Children's perspective of quality of life in epilepsy

Suchergebnisse filtern